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NCT01110343 · ClinicalTrials.gov registry record · NA
Conventional vs Mindfulness Intervention in Parents of Children With Disabilities
A NA study, sponsored by Vanderbilt University.
- Completed
- Registry status
- NA
- Development phase
- 243
- Enrollment target
NCT01110343: Completed NA study, sponsored by Vanderbilt University.
NCT01110343 is a NA study that has completed, run by Vanderbilt University. The registered enrollment target is 243 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01110343, a NA study, has completed, sponsored by Vanderbilt University.
- COMPLETED
- Registry status
- NA
- Development phase
- 243 participants
- Enrollment target
Study Summary
This application compares the effectiveness of a conventional Parent Group intervention to Mindfulness- Based Stress Reduction (MBSR) in parents of children with autism spectrum disorders (ASD) and other disabilities. Parent groups are widely-used to provide information, emotional support, education and advocacy. MBSR is efficacious for people with medical, psychiatric or other concerns, and teaches stress reduction through mindfulness training and practice. In contrast to conventional parent groups, the investigators' studies suggest that mindfulness-based interventions may be particularly effective in reducing stress and improving the health and mental health of parents of children with disabilities. The investigators will assess parent factors that may correlate with intervention efficacy in the 2 treatment arms.
Primary Outcome
Parenting Stress Index standard scores will show treatment effects of intervention by day one of week six of active intervention phase.
Interventions
- BEHAVIORAL mindfulness intervention
- BEHAVIORAL Conventional parent Support Group
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 243 participants |
| Start Date | 2010-02 |
| Est. Completion | 2013-01 |
| Phase | NA |
What the finished NCT01110343 record still lists
NCT01110343 is an interventional study that assigns participants to a tested intervention. The registered 243 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (83% lower).
The record links to 0 conditions, and to 2 interventions - of which mindfulness intervention is the first listed.
NCT01110343 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01110343 about?
NCT01110343 is a clinical study titled "Conventional vs Mindfulness Intervention in Parents of Children With Disabilities". This application compares the effectiveness of a conventional Parent Group intervention to Mindfulness- Based Stress Reduction (MBSR) in parents of children with autism spectrum disorders (ASD) and other disabilities. Parent groups are widely-used to provide information, emotional support, education...
What is the current status of trial NCT01110343?
This trial is currently completed. It is a NA study. The enrollment target is 243 participants. The study started on 2010-02. Estimated completion is 2013-01.
What interventions are being tested in trial NCT01110343?
The interventions under investigation include: mindfulness intervention (BEHAVIORAL), Conventional parent Support Group (BEHAVIORAL).
Who is sponsoring clinical trial NCT01110343?
This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01110343's enrollment target sits among peer trials
243 438th of 2000 higher than 1,562 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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